A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710116



Internal ID133782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65011042..65011066hg38UCSC Ensembl
chr16:65044945..65044969hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546288
Supporting Variants
Samples
Known GenesCDH11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710116
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.054815


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